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S W Scherer

Showing results (91-100 of 164) with videos related to

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Genomics|March 15, 1994
Mapping the human growth hormone-releasing hormone receptor (GHRHR) gene to the short arm of chromosome 7 (7p13-p21) near the epidermal growth factor receptor (EGFR) geneN C Vamvakopoulos, J Kunz, U Olberding, et al.
Oncogene|June 19, 1997
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomasM I Edelson, S W Scherer, L C Tsui, et al.
Blood|March 15, 1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemiasK Fischer, S Fröhling, S W Scherer, et al.
Human Molecular Genetics|June 1, 1993
Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 regionS W Scherer, J M Rommens, S Soder, et al.
Genomics|January 25, 2000
Chromosomal localization of phospholipase A2 activating protein, an Ets2 target gene, to 9p21B G Beatty, S Qi, M Pienkowska, et al.
Leukemia|April 1, 1996
Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)S Tosi, J Harbott, O A Haas, et al.
Neurology|December 10, 2003
Skin biopsy in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsD M Andrade, C A Ackerley, T S C Minett, et al.
Journal of Medical Genetics|March 25, 2006
An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene clusterJ B Vincent, S I Horike, S Choufani, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
American Journal of Human Genetics|January 13, 2000
Involvement of the HLXB9 homeobox gene in Currarino syndromeE Belloni, G Martucciello, D Verderio, et al.
Pageof 17

Showing results (91-100 of 164) with videos related to

Sort By:
Pageof 17
Genomics|March 15, 1994
Mapping the human growth hormone-releasing hormone receptor (GHRHR) gene to the short arm of chromosome 7 (7p13-p21) near the epidermal growth factor receptor (EGFR) geneN C Vamvakopoulos, J Kunz, U Olberding, et al.
Oncogene|June 19, 1997
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomasM I Edelson, S W Scherer, L C Tsui, et al.
Blood|March 15, 1997
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemiasK Fischer, S Fröhling, S W Scherer, et al.
Human Molecular Genetics|June 1, 1993
Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 regionS W Scherer, J M Rommens, S Soder, et al.
Genomics|January 25, 2000
Chromosomal localization of phospholipase A2 activating protein, an Ets2 target gene, to 9p21B G Beatty, S Qi, M Pienkowska, et al.
Leukemia|April 1, 1996
Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)S Tosi, J Harbott, O A Haas, et al.
Neurology|December 10, 2003
Skin biopsy in Lafora disease: genotype-phenotype correlations and diagnostic pitfallsD M Andrade, C A Ackerley, T S C Minett, et al.
Journal of Medical Genetics|March 25, 2006
An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene clusterJ B Vincent, S I Horike, S Choufani, et al.
Human Molecular Genetics|April 18, 1998
Detection of a homozygous four base pair deletion in the protein X gene in a case of pyruvate dehydrogenase complex deficiencyM Ling, G McEachern, A Seyda, et al.
American Journal of Human Genetics|January 13, 2000
Involvement of the HLXB9 homeobox gene in Currarino syndromeE Belloni, G Martucciello, D Verderio, et al.
Pageof 17